Your browser doesn't support javascript.
loading
Successful Generation of Human Induced Pluripotent Stem Cell Lines from Blood Samples Held at Room Temperature for up to 48 hr.
Agu, Chukwuma A; Soares, Filipa A C; Alderton, Alex; Patel, Minal; Ansari, Rizwan; Patel, Sharad; Forrest, Sally; Yang, Fengtang; Lineham, Jonathan; Vallier, Ludovic; Kirton, Christopher M.
Afiliação
  • Agu CA; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK. Electronic address: ac17@sanger.ac.uk.
  • Soares FA; Wellcome Trust-Medical Research Council Cambridge Stem Cell Institute, Anne McLaren Laboratory for Regenerative Medicine and Department of Surgery, University of Cambridge, Cambridge CB2 0QQ, UK.
  • Alderton A; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Patel M; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Ansari R; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Patel S; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Forrest S; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Yang F; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Lineham J; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Vallier L; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK; Wellcome Trust-Medical Research Council Cambridge Stem Cell Institute, Anne McLaren Laboratory for Regenerative Medicine and Department of Surgery, University of Cambridge, Cambridge CB2 0QQ, UK.
  • Kirton CM; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Stem Cell Reports ; 5(4): 660-71, 2015 Oct 13.
Article em En | MEDLINE | ID: mdl-26388286
ABSTRACT
The collection sites of human primary tissue samples and the receiving laboratories, where the human induced pluripotent stem cells (hIPSCs) are derived, are often not on the same site. Thus, the stability of samples prior to derivation constrains the distance between the collection site and the receiving laboratory. To investigate sample stability, we collected blood and held it at room temperature for 5, 24, or 48 hr before isolating peripheral blood mononuclear cells (PBMCs) and reprogramming into IPSCs. Additionally, PBMC samples at 5- and 48-hr time points were frozen in liquid nitrogen for 4 months and reprogrammed into IPSCs. hIPSC lines derived from all time points were pluripotent, displayed no marked difference in chromosomal aberration rates, and differentiated into three germ layers. Reprogramming efficiency at 24- and 48-hr time points was 3- and 10-fold lower, respectively, than at 5 hr; the freeze-thaw process of PBMCs resulted in no obvious change in reprogramming efficiency.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucócitos Mononucleares / Células-Tronco Pluripotentes Induzidas / Técnicas de Reprogramação Celular Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucócitos Mononucleares / Células-Tronco Pluripotentes Induzidas / Técnicas de Reprogramação Celular Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article